PIP, DLA and AA
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PIP

jeannettestevensonjeannettestevenson Member Posts: 9 Listener
We were really worried about my husband being changed from DLA to PIP. It took forever. We received the letter in July and returned the form almost immediately. Lousy GP refused to help. Interview was October 4th. The decision came thru in late November. He's been upped to enhanced daily living. Keeps the enhanced movilify and therefore the mutability car and the award is for 10 years. DLA finishes 17th December. PIP starts 18th December. It's been a nightmare bit all came good. Now I'm in the middle of as I've been diagnosed with MS. Not as worried as anything I get will be extra and I have lots of support from MS nurse and neurologist etc. Hope everyone else has had positive results too

Replies

  • jeannettestevensonjeannettestevenson Member Posts: 9 Listener
    We were really worried about my husband being changed from DLA to PIP. It took forever. We received the letter in July and returned the form almost immediately. Lousy GP refused to help. Interview was October 4th. The decision came thru in late November. He's been upped to enhanced daily living. Keeps the enhanced movilify and therefore the mutability car and the award is for 10 years. DLA finishes 17th December. PIP starts 18th December. It's been a nightmare bit all came good. Now I'm in the middle of as I've been diagnosed with MS. Not as worried as anything I get will be extra and I have lots of support from MS nurse and neurologist etc. Hope everyone else has had positive results too
  • pollyanna1052pollyanna1052 Member Posts: 1,999 Disability Gamechanger
    Hi Jeanette.

    Great to hear your hubby got the full award. Just got mine too, after great anxiety going from DLA to PIP. What a relief!

    Sad to read about your diagnosis.

    I was wrongly diagnosed with PPMS for several years so do know a bit about it.

    Hope you are receiving all the help you need.

    lots of love Pollyxxx
  • jeannettestevensonjeannettestevenson Member Posts: 9 Listener
    Thank you Polly. I have great support and have had for possibly 20-25 years. Also have 2 new active lesions on my brain I have PPMS. Rather a shock when I thought it was a trapped nerve. More so when they found a tomour in my lung. But they've cut that and half my lung out so onwards and upwards ☺
  • woodbinewoodbine Member Posts: 2,994 Disability Gamechanger
    Always good to hear positive outcomes well done
    my advice is given freely and is correct to the best of my knowledge.
  • Chloe_ScopeChloe_Scope Scope Posts: 10,662 Disability Gamechanger
    Really glad it was a positive outcome @jeannettestevenson! I hope it's the same result for yourself. If there is anything we can do to help then please do let us know. :)
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  • Adrian_ScopeAdrian_Scope Testing Team, Community Team Posts: 7,949 Scope community team
    That's brilliant news @jeannettestevenson! Best of luck with your own application too. 
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